Evidence map›Paper›PMID 17097219›Full record

ArticleMolecular and cellular endocrinology2007

Distal regulatory elements are required for Fshr expression, in vivo.

Brian P Hermann, Kaori I Hornbaker, Rengasamy R M Maran, Leslie L Heckert

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  9. Review
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  12. Transcriptional regulation of the FSH receptor: new perspectives.Molecular and cellular endocrinology · 2007
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Brian P HermannDepartment of Molecular and Integrative Physiology, University of Kansas Medical Center, 3901 Rainbow Boulevard, Kansas City, KS 66160, USA.
Kaori I Hornbaker
Rengasamy R M Maran
Leslie L Heckert
University of Kansas Medical Center · US

Funding

UTERINE VASCULAR CHANGES &ANGIOGENESIS DURING IMPLANTATIONU54HD033994 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI TERRANOVA, PAUL FRANK · 2001 to 2005
$5.6M
TRANSCRIPTIONAL REGULATION OF THE FSH RECEPTORR29HD035217 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HECKERT, LESLIE L · 1998 to 2002
$327k
SF1 &CREB: GONADAL ROLES BY A NEW TRANSGENIC APPROACHR03HD035871 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI HECKERT, LESLIE L · 1998 to 1999
–
NICHD NIH HHS HD35217NICHD NIH HHS R29 HD035217NICHD NIH HHS U54 HD033994NICHD NIH HHS U54-HD33994
6 · The paper itself

Abstract

The gonadotropin follicle-stimulating hormone (FSH) is required for initiation and maintenance of normal gametogenesis and acts through a specific, cell-surface receptor (Fshr) present only on Sertoli and granulosa cells in the gonads. Despite extensive examination of the transcriptional mechanisms regulating Fshr, the sequences directing its expression to these cells remain unidentified. To establish the minimal region necessary for Fshr expression, we generated transgenic mice carrying a yeast artificial chromosome (YAC) that contained 413 kilobases (kb) of the rat Fshr locus (YAC60). Transgene expression, as determined by RT-PCR, was absent from immature testis and Sertoli cells, limited to germ cells of the adult testis, and never observed in the ovary. While the data is limited to only one transgenic line, it suggests that the 413kb region does not specify the normal spatiotemporal expression pattern of Fshr. Comparative genomics was used to identify potential distal regulatory elements, revealing seven regions of high evolutionary conservation (>80% identity over 100bp or more), six of which were absent from the transgene. Functional examination of the evolutionary conserved regions (ECRs) by transient transfection revealed that all of the ECRs had modest transcriptional activity in Sertoli or myoid cells with two, ECR4 and ECR5, showing differential effects in expressing and non-expressing cells. These data reveal that distal regulatory regions (outside the 413kb in YAC60) are required for appropriate temporal and spatial Fshr expression and implicate the identified ECRs in transcriptional regulation of Fshr.

Indexed as

AnimalsBase SequenceChromosome MappingChromosomes, Artificial, YeastConserved SequenceEvolution, MolecularGene Expression ProfilingGene Expression RegulationHumansIntegrasesMiceMice, TransgenicRatsReceptors, FSHRecombination, GeneticRegulatory Sequences, Nucleic AcidCre recombinaseIntegrasesReceptors, FSHRNA, Messenger

Identifiers

PMID17097219
PMCPMC1764205
OpenAlexW2021736159

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.